Methanesulfonyl chloride → 76345-45-4
Reaction equation
[CH3:1][S:2](Cl)(=[O:4])=[O:3].[N+:6]([C:9]1[CH:14]=[C:13]([NH2:15])[CH:12]=[CH:11][C:10]=1[NH2:16])([O-:8])=[O:7]>N1C=CC=CC=1>[NH2:16][C:10]1[CH:11]=[CH:12][C:13]([NH:15][S:2]([CH3:1])(=[O:4])=[O:3])=[CH:14][C:9]=1[N+:6]([O-:8])=[O:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methanesulfonyl chloride (11.5 g, 0.1 mmol) was added gradually over 3 min to a solution of 2-nitrobenzene-1,4-diamine (15.3 g) in pyridine (70 ml). The temperature of the mixture rose to ca. 70° C. The solution was set aside for 10 min, and then refluxed for 15 min. The pyridine was evaporated under reduced pressure, and the residue was recrystallized from ethanol (with charcoal) to give the product as white solid.
Workup
- customrose to ca. 70° C
- temperaturerefluxed for 15 min
- customThe pyridine was evaporated under reduced pressure
- customthe residue was recrystallized from ethanol (with charcoal)
Sources & evidence
- ORD record
- ord-10eeb3b8175a404fbb739865ea5f53ab
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09193717B2
Reaction notes
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